atrial heart septal defect 7

Summary
Synonym
  • ASD with or without atrioventricular conduction defects
  • atrial septal defect 7, with or without AV conduction defects
  • atrial septal defect-atrioventricular conduction defects syndrome
Definition
An atrial heart septal defect that has_material_basis_in heterozygous mutation in the NKX2-5 gene on chromosome 5q35.
Super Class
atrial heart septal defect autosomal dominant disease
External Links
Disease Ontology
DOID:0110112
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 31 - 38 of 38 in total
Gene ID Gene Symbol Description Source
29940 DSE dermatan sulfate epimerase
55997 CFC1 cryptic, EGF-CFC family member 1
64132 XYLT2 xylosyltransferase 2
79087 ALG12 ALG12 alpha-1,6-mannosyltransferase
92579 G6PC3 glucose-6-phosphatase catalytic subunit 3
113189 CHST14 carbohydrate sulfotransferase 14
126792 B3GALT6 beta-1,3-galactosyltransferase 6
145173 B3GLCT beta 3-glucosyltransferase
Related Glycoprotein
Displaying entry 31 - 31 of 31 in total
UniProt ID Protein Name Source
Q9Y625 Glypican-6

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024